반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([O:9][CH3:10])=[CH:5][C:4]=1B(O)O.Br[C:15]1[CH:16]=[C:17]([CH:19]=[CH:20][CH:21]=1)[NH2:18].C([O-])([O-])=O.[Na+].[Na+]>COCCOC.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([O:9][CH3:10])=[CH:5][C:4]=1[C:15]1[CH:21]=[CH:20][CH:19]=[C:17]([NH2:18])[CH:16]=1참가 물질
실험 절차
2,5-dimethoxyphenyl boronic acid (0.126 g, 0.693 mmol) and 3-bromoaniline (0.05 mL, 0.462 mmol) were combined in DME (2 mL) in a flame-dried, round-bottom flask. Na2CO3 (2M, 0.485 mL, 0.970 mmol) and Pd(PPh3)4 (0.017 g, 0.014 mmol) were added to the stirred solution. The reaction was refluxed overnight under argon flow, and subsequently cooled to room temperature. The solvent was removed under vacuum and the resulting residue was resuspended in H20 and extracted with CH2Cl2. The organic phase was dried over MgSO4 and concentrated under vacuum. The crude product was purified by silica column chromatography (0-20% EtOAc/hexanes). The purification was monitored by TLC. The solvent was removed under vacuum from fractions containing product, resulting in 0.091 g in 91% yield.
후처리
- temperatureThe reaction was refluxed overnight under argon flow
- customThe solvent was removed under vacuum
- extractionextracted with CH2Cl2
- dry with materialThe organic phase was dried over MgSO4
- concentrationconcentrated under vacuum
- customThe crude product was purified by silica column chromatography (0-20% EtOAc/hexanes)
- customThe purification
- customThe solvent was removed under vacuum from fractions
- additioncontaining product
- customresulting in 0.091 g in 91% yield
출처 및 근거
- ORD 기록
- ord-a4c297573b324cb986a1679e0f331f09
- 출처 데이터셋
- uspto-grants-2014_02
- 특허 번호
- US08642788B2
연결된 노트
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